Inhibition caused by adsorption of organic micropollutants (MPs) on PES@CoFe2O4 polymeric ultrafiltration membranes and the enhanced MPs degradation by a continuous pH regulation

In this work, catalytic membranes were fabricated by blending CoFe2O4 catalysts into polyethersulfone (PES) and then used to treat naproxen with the addition of peroxymonosulfate (PMS). It was found that the addition of PMS results in a decrease in pH, which increases the adsorption of naproxen. This often overlooked phenomenon is demonstrated here to have an important role since the adsorption of naproxen on the polymeric matrix and catalytic particles decreases the degradation efficiency of naproxen. To verify this hypothesis and rule out the decrease in pH after the addition of pH, two ways of controlling the pH of the naproxen solution were compared: adjusting pH before and after the addition of PMS, respectively. Our results indicate that in the batch experiment, adjusting the pH of naproxen solution after adding PMS led to a dramatic 23-fold increase in the kinetic constant of the naproxen oxidation (0.42/min, pH6) compared to when pH was adjusted before adding PMS (0.018/min, pH 6). This enhancement in the overall kinetics was attributed to the elimination of the inhibition caused by MPs adsorption at low pH. In a dead-end cell, the catalytic membranes with 2.0 % of CoFe2O4 achieved quantitative conversion of naproxen, bisphenol A, and atrazine, with values of 98 %, 97 %, and 74 %, respectively, demonstrating the efficacy of this approach to convert multitype of MPs in wastewater streams. In a reusability study, the naproxen removal of the catalytic membranes with 2.0 % of CoFe2O4 decreased by 81 % and 45 % after 5 rounds in the batch experiment and dead-end cell, respectively. However, with a chemical cleaning process between each round, the degradation efficiency can be effectively recovered, proving the negative effects of the adsorption of MPs or their intermediates during the SR-AOPs. Our work demonstrates that pH in SR-AOPbased catalytic membrane processes determined both the reaction rate and the adsorption of MPs or their intermediates on the membrane and its reactive sites. We envision that these results will be valuable in developing efficient catalytic membranes for the treatment of MPs in wastewater streams.